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Aldep (Alprazolam)
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Aldep

Aldep is commonly used to treat anxiety and panic disorders. It falls into a category of medications called benzodiazepines. They are known to affect the central nervous system components and produce a calming effect, thus decreasing brain activity.

Other names for this medication:
Aldep, Aleez, Almac, Alprac, Alprasan, Alprowon, Alsert, Altin, Altok, Alzam, Alzex, Alzopam, Alzorix, Anxico, Anxit, Avizolem, Balzam, Deproz, Eurolam, Exprex, Ezoprax, Faxtin, Finezol, Fludep, Fluzolam, Hiprazole, Kaprolam, Mentolift, Nexlpra, Pizolam, Pranol, Prozam, Richpram, Romipraz, Rozin, Sertamax, Silam, Suzilam, Tensfree, Tensyl, Tensyn, Texidep, Visram, Zeprax, Zomark, Zopax

Similar Products:
Sovaldi, Celexa, Zyprexa, Micardis, Persantine, Compivas, Versamid, Orizal, Psycholanz, Phytoral, Periran, Alpan, Dynoxytet,

Also known as: Alprazolam

Description

Aldep is a benzodiazepine (ben-zoe-dye-AZE-eh-peen). Alprazolam affects chemicals in the brain that may be unbalanced in people with anxiety. Aldep is used to treat anxiety disorders, panic disorders, and anxiety caused by depression.

You should not use Aldep if you have narrow-angle glaucoma, if you also take itraconazole or ketoconazole, or if you are allergic to Aldep or similar medicines (Valium, Ativan, Tranxene, and others).

Alprazolam may be habit-forming. Misuse of habit-forming medicine can cause addiction, overdose, or death.

Do not drink alcohol while taking Aldep. This medication can increase the effects of alcohol. Alprazolam may be habit-forming and should be used only by the person for whom it was prescribed. Keep the medication in a secure place where others cannot get to it.

Dosage

This section provides information on the proper use of a number of products that contain alprazolam. It may not be specific to Aldep. Please read with care.

Take this medicine only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered. If too much of this medicine is used for a long time, it may become habit-forming (causing mental or physical dependence) or cause an overdose.

This medicine should come with a Medication Guide. Read and follow the instructions carefully. Ask your doctor if you have any questions.

Swallow the extended-release tablet or tablet whole with a full glass of water. Do not break, crush, or chew it.

If you are using the orally disintegrating tablet, make sure your hands are dry before you handle the tablet. Do not remove the tablets from the bottle until you are ready to take it. Place the tablet immediately on the top of your tongue. It should melt quickly and be swallowed with saliva.

If you are using the oral liquid, measure the dose with a marked measuring spoon, oral syringe, or medicine cup.

Do not eat grapefruit or drink grapefruit juice while you are using this medicine.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For anxiety: For oral dosage forms (solution, tablets, or orally disintegrating tablets): Adults—At first, 0.25 to 0.5 milligram (mg) 3 times a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 4 mg per day. Older adults—At first, 0.25 mg 2 or 3 times a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor. For panic disorder: For oral dosage form (extended-release tablets): Adults—At first, 0.5 to 1 milligram (mg) taken in the morning once a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 10 mg per day. Older adults—At first, 0.5 mg taken in the morning once a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor. For oral dosage forms (solution, tablets, or orally disintegrating tablets): Adults—At first, 0.5 milligram (mg) 3 times a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 10 mg per day. Older adults—At first, 0.25 mg 2 or 3 times a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor.

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of alprazolam can be fatal.

Overdose symptoms may include extreme drowsiness, confusion, muscle weakness, loss of balance or coordination, feeling light-headed, and fainting.

Storage

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

It is very important to protect the orally disintegrating tablets from moisture. Remove and throw away any cotton packaging from the medicine bottle when you first use the medicine.

Detailed Aldep XR dosage information

Side effects

The most common side effects associated with Aldep are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Keep a list of all the products you use (including prescription/nonprescription drugs and herbal products) and share it with your doctor and pharmacist. Do not start, stop, or change the dosage of any medicines without your doctor's approval.Some products that may interact with this drug include: kava, sodium oxybate.Other medications can affect the removal of Aldep from your body, which may affect how Aldep works. Examples include azole antifungals (such as itraconazole, ketoconazole), cimetidine, certain anti-depressants (such as fluoxetine, fluvoxamine, nefazodone), drugs to treat HIV (delavirdine, protease inhibitors such as indinavir), macrolide antibiotics (such as erythromycin), rifamycins (such as rifabutin), St. John's wort, drugs used to treat seizures (such as carbamazepine, phenytoin), among others.Tell your doctor or pharmacist if you also take drugs that cause drowsiness such as: certain antihistamines (such as diphenhydramine), medicine for sleep or anxiety (such as diazepam, zolpidem), muscle relaxants, narcotic pain relievers (such as codeine), psychiatric medicines (such as chlorpromazine, risperidone, amitriptyline, trazodone).Check the labels on all your medicines (such as cough-and-cold products) because they may contain ingredients which cause drowsiness. Ask your pharmacist about the safe use of those products.Cigarette smoking decreases blood levels of this medication. Tell your doctor if you smoke or if you have recently stopped smoking.

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BER down-regulates anti-apoptotic protein Bcl-2 levels and up-regulates pro-apoptotic protein Bax expressions in MDA-MB-231 and MDA-MB-435S cells. Cyclone aims at facilitating the use of BioCyc, a collection of Pathway/Genome Databases (PGDBs). The human tissue distribution of the nineteen known human regulators of G-protein signaling (RGS) is described. Single doses of niridazole (which suppress cell-mediated immune responses) had no effect whatsoever on the most strongly inhibited of the primary antibody responses, that to alum-precipitated polymerized human serum albumin. Ribonucleoprotein particles (RNPs) of rice hoja blanca virus (RHBV) were purified and used for electron microscopic analysis and antibody production. In mouse models modulation of T cell function ameliorated not only adipose inflammation but also systemic insulin resistance induced by obesity. These anticholinesterases caused gradual bronchoconstriction as indicated by a diminution in tidal air volume, a reduction in compliance and an increase in expiratory resistance. This study portrays the importance of single cell observations pertaining to the host-parasite relationship. Effect of hypertension on vectroelectrocardiogram with a special reference to the ventricular gradient.

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Comparison of thelotomy and theloscopic triangulation for the treatment of distal teat obstructions in dairy cows--a retrospective study (1994-1998). Effect of L-fucose and fucose-rich polysaccharides on elastin biosynthesis, in vivo and in vitro. Capacity of multidrug-resistant clinical isolates of Acinetobacter baumannii to form biofilm and adhere to epithelial cell surfaces. This study considers variation in fluorescence intensity (FI) under various coagulation conditions to assess the mechanism by which humic acids and phosphate react with aluminum ions. A high clinico-epidemiological effectiveness ws approved for 10-days administration of the Natrii nucleinas in persons with clinic manifestations of grip and other respiratory infections at the moment of vaccination. In this group of lung transplant recipients, HRCT and V/Q scanning, as well as analysis of MMEF, did not add information that was clinically more useful than FEV1 for the early identification of chronic rejection. The predominating majority of the strains were resistant to rifampicin, amoxycillin and phosphomycin. There was no significant decline in fatal injuries to agricultural workers in the study decade.

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Use of a panel of congenic strains to evaluate differentially expressed genes as candidate genes for blood pressure quantitative trait loci. Plasma levels of partly deficient or asialotransferrin increase in chronically drinkers. Reorganization in apo- and holo-beta-lactoglobulin upon protonation of Glu89: molecular dynamics and pKa calculations. Taken together, our data suggest that numerous genes may influence ACE activity. Male rats were given footshocks in a distinctive context and later tested using freezing as the behavioral measure and compared with no-shock and no-retention-test control groups. Using this approach, not only the separation of LSD from the tablet extract was achieved, but on-line spectra were readily distinguishable and could be unambiguously assigned. These findings provide the first evidence for the presence of a DSIP-related peptide in fish.

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Analysis of thymus lipids, at various time intervals following irradiation, showed a threefold increase of triglycerides at 24 hours. In the assay, three compounds (midazolam, nifedipine, and testosterone) were compared as CYP3A probe substrates. Dystopic dysplastic kidney with ectopic ureter: improved localization by fusion of MR urography and (99m)Tc-DMSA SPECT datasets. On this basis, incorporating genotypic resistance assays into the clinical management of HIV patients experiencing first treatment failure is not a sufficiently evidence-based practice. Multiple doses of sitagliptin, a selective DPP-4 inhibitor, do not meaningfully alter pharmacokinetics and pharmacodynamics of warfarin. Cyclic-AMP acting through protein kinase A stimulated promoter recruitment of CCAAT-enhancer binding protein beta, nuclear amaryl maximum dose factor-Y and RNA polymerase II while depleting the promoter of cyclic-AMP response element binding protein. In LapDS, both the quantity of food ingested and the efficiency of digestion are reduced.

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Insulin dependent diabetes mellitus accompanied by nephrocalcinosis and renal failure. The serum level of leptin in infants with acarbose 50 mg asthma after RSV infected was higher than that in healthy and non-asthma children. The major determinants of the extent of remodelling are infarct size and patency of the infarct-related artery. The challenges for undertaking this approach have three components: data integration, risk assessment tasks, and risk decision-making. Therefore, membrane toxicity could be manifested as membrane blocking and membrane expansion. Postnatal changes in the expressions of serotonin 1A, 1B, and 2A receptors in ten brain stem nuclei of the rat: implication for a sensitive period.

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Interpretation of the effect of reduction of soliton interaction by bandwidth-limited amplification. As a result we can show that free energies are less sensitive (than enthalpy or entropy) to the small structural variations of guest molecules. Estimating individual thyroid doses for a case-control study of childhood thyroid cancer in Bryansk Oblast, Russia. The treatment of primary malignant fibrous histiocytomas of the gallbladder is surgery. Mating-competent opaque cells then release pheromone that induces polarization, a G1 block and conjugation tube formation in opaque cells of opposite mating type. On dose bactrim in renal failure plastic middle ear operations with particular attention to the cavum minor technique. Children aged 0 to 15 years who were admitted to a hospital with S pneumoniae isolated from blood, cerebrospinal fluid, or deep aspirate sample. UDP-glucuronosyltransferase transcripts were determined by polymerase chain reaction. Age-dependent impairment of coronary collateral development in humans.

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